Allele Registry

Canonical Allele Identifier: PA645380267

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000776440

RCV002230121

RCV002508935

RCV003446065

ClinVar Variation:

410487

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ala494Ser	CA067740 NM_000179.3:c.1480G>T